Budesonide
- Product NDC
- 60687-645
- 11-digit product format
- 606870645
- Labeler code
- 60687
- Product ID
- 60687-645_e4bc6014-cf69-2182-e053-2a95a90ac873
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- INHALANT
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA205710
- Marketing category
- ANDA
- Marketing start
- 2022-07-20
- Marketing end
- 0000-00-00
- Substance
- BUDESONIDE
- Active strength
- 0 mg/2mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-645-83 | 60687064583 | 30 POUCH in 1 CARTON (60687-645-83) > 1 AMPULE in 1 POUCH (60687-645-79) > 2 mL in 1 AMPULE | 30 pouch | 2022-07-20 | 0000-00-00 | No | No | Current |